TY - JOUR
T1 - The effect of sepsis and its inflammatory response on mechanical clot characteristics
T2 - a prospective observational study
AU - Davies, Gareth R.
AU - Pillai, Suresh
AU - Lawrence, Matthew
AU - Mills, Gavin M.
AU - Aubrey, Robert
AU - D’Silva, Lindsay
AU - Battle, Ceri
AU - Williams, Rhodri
AU - Brown, Rowan
AU - Thomas, Dafydd
AU - Morris, Keith
AU - Evans, Phillip Adrian
N1 - Publisher Copyright:
© 2016, Springer-Verlag Berlin Heidelberg and ESICM.
PY - 2016/9/3
Y1 - 2016/9/3
N2 - Purpose: Sepsis and its progression are known to have a major influence on the coagulation system. Current coagulation tests are of limited use when assessing coagulation in sepsis patients. This study aims to assess the potential for a new functional biomarker of clot microstructure, fractal dimension, to identify changes in the mechanical properties of clot microstructure across the sepsis spectrum (sepsis, severe sepsis and septic shock). Methods: A total of 100 patients that presented acutely to a large teaching hospital were included in this prospective observational study (50 sepsis, 20 severe sepsis and 30 septic shock) against a matched control of 44 healthy volunteers. Fractal analysis was performed, as well as standard markers of coagulation, and six plasma markers of inflammation. Results: Fractal dimension was significantly higher in the sepsis and severe sepsis groups than the healthy control (1.78 ± 0.07 and 1.80 ± 0.05, respectively vs 1.74 ± 0.03) (p < 0.001), indicating a significant increase in mechanical clot strength and elasticity consistent with a hypercoagulable state. Conversely, fractal dimension was significantly lower in septic shock (1.66 ± 0.10, p < 0.001), indicating a significant reduction in mechanical clot strength and functionality consistent with a hypocoagulable state. This corresponded with a significant increase in the inflammatory response. Conclusions: This study confirms that clot microstructure is significantly altered through the various stages of sepsis. Of particular importance was the marked change in clot development between severe sepsis and septic shock, which has not been previously reported.
AB - Purpose: Sepsis and its progression are known to have a major influence on the coagulation system. Current coagulation tests are of limited use when assessing coagulation in sepsis patients. This study aims to assess the potential for a new functional biomarker of clot microstructure, fractal dimension, to identify changes in the mechanical properties of clot microstructure across the sepsis spectrum (sepsis, severe sepsis and septic shock). Methods: A total of 100 patients that presented acutely to a large teaching hospital were included in this prospective observational study (50 sepsis, 20 severe sepsis and 30 septic shock) against a matched control of 44 healthy volunteers. Fractal analysis was performed, as well as standard markers of coagulation, and six plasma markers of inflammation. Results: Fractal dimension was significantly higher in the sepsis and severe sepsis groups than the healthy control (1.78 ± 0.07 and 1.80 ± 0.05, respectively vs 1.74 ± 0.03) (p < 0.001), indicating a significant increase in mechanical clot strength and elasticity consistent with a hypercoagulable state. Conversely, fractal dimension was significantly lower in septic shock (1.66 ± 0.10, p < 0.001), indicating a significant reduction in mechanical clot strength and functionality consistent with a hypocoagulable state. This corresponded with a significant increase in the inflammatory response. Conclusions: This study confirms that clot microstructure is significantly altered through the various stages of sepsis. Of particular importance was the marked change in clot development between severe sepsis and septic shock, which has not been previously reported.
KW - Biomarkers
KW - Clot microstructure
KW - Coagulation
KW - Sepsis
UR - http://www.scopus.com/inward/record.url?scp=84984908643&partnerID=8YFLogxK
U2 - 10.1007/s00134-016-4496-z
DO - 10.1007/s00134-016-4496-z
M3 - Article
C2 - 27592210
AN - SCOPUS:84984908643
SN - 0342-4642
VL - 42
SP - 1990
EP - 1998
JO - Intensive Care Medicine
JF - Intensive Care Medicine
IS - 12
ER -